| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197453239-197453571 | Rare:113 | ||||
| chr2:197499801-197500449 | Common:1; Rare:249; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199911136-199911451 | Rare:112 | ||||
| chr2:200510040-200510263 | Common:1; Rare:69 | ||||
| chr2:200811408-200811580 | Common:1; Rare:55 | ||||
| chr2:200889005-200889445 | Common:3; Rare:142 | ||||
| chr2:200963630-200963914 | Common:1; Rare:71 | ||||
| chr2:201071617-201072047 | Rare:91 | ||||
| chr2:201451450-201451832 | Common:2; Rare:97 | ||||
| chr2:201642633-201642770 | Rare:68 | ||||
| chr2:201643449-201643493 | Rare:14; Clinvar:2 | ||||
| chr2:202238447-202238630 | Rare:64; Clinvar:1 | ||||
| chr2:202265662-202265814 | Rare:59 | ||||
| chr2:202911898-202912291 | Common:2; Rare:108 | ||||
| chr2:206159362-206159982 | Common:4; Rare:183; Clinvar (benign):1 |